Bard recalls 5625240 DuoGlide Short-Term Straight Dialysis Catheters due to lidocaine ampoules being manufactured under deficient practices. Affected units have UDI-DI code 00801741042119 and lot number REKY0255.
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard is recalling specific short-term dialysis catheters because the lidocaine ampoules used in their production were made with deficient manufacturing practices. This could pose a risk to patients using the catheters for dialysis treatments.
The lidocaine ampoules used in manufacturing the catheters were produced under deficient practices. This could lead to improper drug delivery during dialysis treatments, potentially causing harm to patients.
Patients using the recalled catheters for short-term dialysis treatments are most at risk. The affected units have a specific UDI-DI code and lot number.
Check for the UDI-DI code 00801741042119 and lot number REKY0255 on the catheter packaging. The product is a 13 Fr Dual-Lumen Short-Term Straight Dialysis Catheter.
Look for the UDI-DI code 00801741042119 and lot number REKY0255 on the catheter packaging.
The lidocaine ampoules used in manufacturing the catheters were produced under deficient practices, which could affect patient safety during dialysis treatments.
The UDI-DI code for the recalled catheter is 00801741042119.
The affected lot number is REKY0255.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2657-2026 — Bard Bard Hello, I own a Bard that is covered by recall Z-2657-2026 from Bard. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.